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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02467257
Other study ID # AlNeelainU
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received June 4, 2015
Last updated June 5, 2015
Start date April 2014
Est. completion date January 2015

Study information

Verified date June 2015
Source Al-Neelain University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether Gum Arabic is effective as fetal hemoglobin inducing agent for sickle cell anemia patients.


Description:

: High level of fetal haemoglobin (Hb F) decreases sickle cell anaemia (SCA) severity and leads to improved survival. Butyrate proved to increase HbF production in vivo and in vitro studies. Nonetheless, its short half-life limited its utilization in clinical practice. Gum Arabic (GA) is edible, dried, gummy exudate from Acacia Senegal tree. GA fermentation by colonic bacteria increases serum butyrate concentrations. The investigators hypothesized regular intake of GA will increase serum butyrate level. The latter will induce fetal hemoglobin production and ameliorate patients' symptoms. 47 patients hemoglobin SS aged 5-42 years, on regular follow up in Military hospital were recruited from April 2014 to January 2015 Patients received dose of G A 30g/day for 12 weeks. Hb F, complete blood count and Erythropoietin level were measured. The main outcome of interest was the level of HbF after 12 weeks.


Recruitment information / eligibility

Status Completed
Enrollment 47
Est. completion date January 2015
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender All
Age group 5 Years to 50 Years
Eligibility Inclusion Criteria:

1. over 5 year old

2. less t5han 50

3. diagnosed with homozygous sickle cell anemia by Hb electrophoresis

Exclusion Criteria:

1. patients received blood transfusion within the last three months or admitted to the hospital within 2 weeks because of Sickle cell anemia -related events or crisis.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Gum Arabic
oral ingestion of 30 gram every day for 12 weeks

Locations

Country Name City State
Sudan Military Hospital Omdurman Khartoum

Sponsors (3)

Lead Sponsor Collaborator
Al-Neelain University Military hospital, Ministry of Higher Education and Scientific Research, Republic of Sudan

Country where clinical trial is conducted

Sudan, 

References & Publications (4)

Ballal A, Bobbala D, Qadri SM, Föller M, Kempe D, Nasir O, Saeed A, Lang F. Anti-malarial effect of gum arabic. Malar J. 2011 May 20;10:139. doi: 10.1186/1475-2875-10-139. — View Citation

Fathallah H, Atweh GF. Induction of fetal hemoglobin in the treatment of sickle cell disease. Hematology Am Soc Hematol Educ Program. 2006:58-62. Review. — View Citation

Kutlar A, Reid ME, Inati A, Taher AT, Abboud MR, El-Beshlawy A, Buchanan GR, Smith H, Ataga KI, Perrine SP, Ghalie RG. A dose-escalation phase IIa study of 2,2-dimethylbutyrate (HQK-1001), an oral fetal globin inducer, in sickle cell disease. Am J Hematol. 2013 Nov;88(11):E255-60. doi: 10.1002/ajh.23533. Epub 2013 Oct 3. — View Citation

Matsumoto N, Riley S, Fraser D, Al-Assaf S, Ishimura E, Wolever T, Phillips GO, Phillips AO. Butyrate modulates TGF-beta1 generation and function: potential renal benefit for Acacia(sen) SUPERGUM (gum arabic)? Kidney Int. 2006 Jan;69(2):257-65. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The primary endpoint of the study will be the level of fetal hemoglobin after three months fetal hemoglobin will be measured each month for three months 12 weeks
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